The incumbent is challenged to provide oversight of the clinical research coordinator and research associate pool and research protocols with an extremely high degree of accuracy, adheres to project timelines, ensures proper quality assurance measures are taken and complies with all regulatory requirements. The Lead must stay current on the understanding of all regulations specific to human research subject protections and informed consent. While the incumbent must be highly organized and tolerant of isolation, this person must also have good interpersonal skills to communicate with research staff, physicians, physician staff, study sponsors, and research participants. This position prepares, submits, and monitors documentation of research program activities while assuring compliance with regulations and protocols. Performs assigned administrative, clinical, and technical duties as directed. Duties include but are not limited to scheduling and consenting participants, coordinator pool training, data entry, assist research area Supervisor and Manager of Clinical Research on staff evaluations and staff career development. Completes other work as requested.
Serves as a Renown Health Lead Clinical Research Coordinator in the Renown Research Office.
This position is challenged to manage a large volume of items while maintaining a high degree of accuracy and efficiency with significant attention to detail. Working knowledge of all regulatory requirements governing IRB guidelines. The position requires strong decision-making, independent judgment, and analytical skills in order to apply federal and state regulations to a variety of situations.
This position provides patient care.
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